Variant report

Variant	rs73778946
Chromosome Location	chr6:149232885-149232886
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs61636972	1.00[EUR][1000 genomes]
rs73778947	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7763394	1.00[EUR][1000 genomes]
rs9485341	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032690	chr6:149206106-149398712	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv464074	chr6:149211090-149242095	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv604844	chr6:149211090-149242095	Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv464075	chr6:149221294-149242095	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv470865	chr6:149221294-149242095	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv604845	chr6:149221294-149242095	Enhancers Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149207800-149237400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr6:149209000-149247600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:149210200-149240200	Weak transcription	Primary B cells from cord blood	blood
4	chr6:149210400-149235000	Weak transcription	Primary B cells from peripheral blood	blood
5	chr6:149211600-149255400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr6:149213200-149233400	Weak transcription	Fetal Heart	heart
7	chr6:149217600-149236800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr6:149225400-149233400	Weak transcription	Colon Smooth Muscle	Colon
9	chr6:149226600-149252800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr6:149226600-149255600	Weak transcription	Ovary	ovary
11	chr6:149227200-149236400	Weak transcription	Fetal Stomach	stomach
12	chr6:149227400-149240400	Weak transcription	Pancreas	Pancrea
13	chr6:149230800-149238000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:149230800-149244600	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr6:149231000-149237000	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr6:149231000-149244200	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr6:149231000-149245400	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr6:149231200-149233400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr6:149231200-149236600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr6:149232200-149234400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr6:149232400-149235000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr6:149232600-149236000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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